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Amla on Metabolic Syndrome, Insulin Sensitivity and Insulin Secretion

Effect of Amla Administration on Metabolic Syndrome, Insulin Sensitivity and Insulin Secretion.

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03633630
Enrollment
28
Registered
2018-08-16
Start date
2019-04-01
Completion date
2022-03-30
Last updated
2022-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Syndrome

Keywords

Amla, Emblica officinalis, Metabolic Syndrome, Insulin Secretion, Insulin Sensitivity

Brief summary

Amla has demonstrated promising effects in the treatment of obesity, dyslipidemia, hypertension, insulin secretion, among others. The above mentioned findings show that Amla has an excellent potential for the prevention and treatment of metabolic syndrome.

Detailed description

A randomized, double-blind, placebo-controlled clinical trial will be conducted in 28 patients, 30-59 years old, with diagnosis of Metabolic Syndrome according with modified International Diabetes Federation criteria. Patients will be randomly assigned to receive Amla (500mg) or homologated placebo orally twice daily, for 90 days. Before and after the intervention, the components of Metabolic Syndrome will be evaluated, waist circumference, blood pressure, levels of fasting glucose, triglycerides, cholesterol high density lipoprotein (C-HDL), total insulin secretion (Insulinogenic index), first phase of insulin secretion (Stumvoll index) and insulin sensitivity (Matsuda index).

Interventions

DRUGAmla

Capsules of 500 mg two times per day before breakfast and dinner a total dose of 1000 mg per day. During 90 days

DRUGPlacebo

Capsules of 500 mg two times per day before breakfast and dinner a total dose of 1000 mg per day. During 90 days

Sponsors

University of Guadalajara
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
30 Years to 59 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed Metabolic Syndrome according to the IDF criteria: * \- - Waist circumference: ≥80 cm (women) ≥90 cm (men), plus two or more of the following: * \- - Fasting glucose ≥ 100 mg/dL to \<126 mg/dL. * \- - Triglycerides ≥150 mg/dL to \<499 mg/dL * \- - HDL-C: Men ≤40 mg/dL, women ≤50 mg/dL * \- - Systolic blood pressure ≥130 to \<140 mmHg * \- - Diastolic blood pressure ≥85 to \<89 mmHg * Body Mass Index between 25 and 34.9 kg/m² * No pharmacological treatment for Metabolic Syndrome

Exclusion criteria

* Pregnancy or breast-feeding * Known allergy to Amla or placebo * History of hepatic, kidney or thyroid disease * Drugs or supplements consumption with proven properties that modify the behavior of the Metabolic Syndrome

Design outcomes

Primary

MeasureTime frameDescription
Waist Circumference (WC)90 daysThe WC will be evaluated after an overnight fast with a flexible tape in the midpoint between the lowest rib and the iliac crest. The value will be expressed in centimeters.
Triglycerides (TGs)90 daysThe blood sample for determining of TGs, will be taken after an overnight fast and with a spectrophotometry method. The value will be expressed on mmol/L.
High-density Lipoprotein Cholesterol (HDL-C)90 daysThe blood sample for determining of HDL-C, will be taken after an overnight fast with a colorimetric method. The value will be expressed on mmol/L.
Fasting Plasma Glucose (FPG)90 daysThe blood sample for determining of FPG, will be taken after an overnight fast and with a spectrophotometry method. The value will be expressed on mmol/L.
Systolic Blood Pressure (SBP)90 daysThe SBP will be evaluated with a digital sphygmomanometer with the subject sited down on a chair after a resting period of 5 minutes on three occasions. The mean of the three measures will be considered as the value of SBP. The value will be expressed on mmHg.
Diastolic Blood Pressure (DBP)90 daysThe DBP will be evaluated with a digital sphygmomanometer with the subject sited down on a chair after a resting period of 5 minutes on three occasions. The mean of the three measures will be considered as the value of DBP. The value will be expressed on mmHg.

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026